Vascularized islets and methods of producing same
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example 1
Generation of 3D Pancreatic Islet Co-Culture System
[0133]Materials and Methods
[0134]Animals: 3 month old C57 black male mice.
[0135]Isolation of mouse pancreatic islets: Adult pancreatic islets were isolated from mice pancreases by using collagenase P (Roche). Briefly, the bile duct was clamped off at its duodenal insertion by using a small bulldog clamp. A total of 5 ml 1.5 mg / ml collagenase was injected into the bile duct, followed by digestion at 37° C. for 15 min. After two centrifugations, islets were handpicked under a stereomicroscope.
[0136]Cell culture: 10-30 mouse pancreatic islets were cultured on PLLA / PLGA scaffold (PLGA, Boehringer Ingelheim Resomer 503H, Ingelheim, Germany, Mn≈25,000 and PLLA, Polysciences, Warrington, Pa., Mn≈300,000) in the presence and absence of fibroblasts and HUVEC for up to three weeks following which they were fixed and embedded in formalin.
[0137]Medium conditions: First co-culture medium conditions were identified—a medium in which the different...
example 2
Role of Endothelial Cells on Pancreatic Islet Survival
[0144]In order to demonstrate the role of endothelial cells on pancreatic islet survival, pancreatic islets were grown with or without endothelial cells.
[0145]Materials and Methods
[0146]The 3D pancreatic islet co-culture system was generated as described for Example 1.
[0147]Results
[0148]Without endothelial cells, the islets deteriorated following 8 days in culture, as can be clearly seen in FIG. 2A. However in islets co-cultured with endothelial cells the islets remained intact and express high levels of insulin even after 21 days (FIGS. 3J-L).
[0149]These preliminary results exhibit the important role of endothelial cells in preserving the morphology and survival of the islets cells.
example 3
Role of 3D Microenvironment on Pancreatic Islet Survival
[0150]To emphasize the role of 3D microenvironment, the identical cell cultures as in Example 2 were grown on tissue plates, a 2D setting.
[0151]Materials and Methods
[0152]The 3D pancreatic islet co-culture system was generated as described for Example 1.
[0153]The 2D pancreatic islet co-culture system was generated essentially as above using 6 well tissue plates (Nunc A / S).
[0154]Results
[0155]The endothelial organization was profoundly different in the 3D and 2D culture settings (FIGS. 3A-L).
[0156]Round clusters and rings were observed in the 2D culture, while the 3D allowed the cells to form elongated interconnecting tubes, forming a vascular network-like structure. Following 8 or 21 days the different cultures were fixed and embedded. Sections were stained for VWF (endothelial marker), and Insulin.
[0157]Conclusions
[0158]The results herein show the importance of a 3D culture system. The presence of endothelial cells forming 3D v...
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